| Tag | Content |
|---|
EnhancerAtlas ID | HS002-09956 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr9:117313930-117315380 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr9:117315320-117315337 | TCAATTCCTAGAAAAAA | - | 6.15 | | KLF4 | MA0039.3 | chr9:117314906-117314917 | CCACACCCTCC | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 117314027 | 117315316 | | chr9 | 117314293 | 117314590 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I114550 | chr9 | 117312897 | 117316577 |
|
Enhancer Sequence | AGCGATCCTC CCACCTTGGC CTCCCAAAGT ACTGGGATTA CAGGCGTAAG CCACTGCACC 60
CAGCCTCACA CACTCTGAAT TATGTGGGGT GGGGTCCTAA CTAACTCACT GAGCCTCCCA 120
AGCCAAACTC AACCGCAGCT ATTCTCCATC CCAAAAGTGG GAAGGAGCTG CCTATTGAGG 180
GAGAGGTGGG CCTTCTTCCC ATTCTCCATC TTCACCTACA AGCTATCCAC TATGCAGGGG 240
CTGCTTGGAG TTTTAACACT GATCCAGTAG CTCACCTGGC TCTTGCCTAA GTAAATTACC 300
TTTCTCCCTT GGGGTTGGGG AGGTGTGGGT CTGGGTGGTG GGCACTGGCT TTACCTCCAG 360
CTCAGCTCCT TCTCTTTGGT CCCGCCTCCC AGGGTTTTAT GTGTCCATAT AACCACTGAC 420
TCAGGGTCAG CTTTTTCCAG TCTAGTGCGT CAGCACAAGT GAGTGATAGA GCCTGAAGGC 480
CATTACTCAG GGGAGGATGG TGGTGAGTCA TCACGAGAGA CTCCTTCCCT AGTCTGGCCA 540
CTCTGCTCCA AGCTGTGCTG GGAGACAGAG AATAATAACA CCTTTTGGAC TGGCCTTTTA 600
AAAATAGAAA CAATGGAGTC TGTGGCTTTA GGAGGAGAGG TCCTGGGAGT CAGAAGCTCA 660
GTCCTGCTAG CTTGTCATTC CTTGGAGGAT GCTGGCTACT ACTTTGCCCA CCGGTAATTG 720
AGGGTGTTGC CCTTGGCCAT TTGGGGTGGG CTTTCTGAGT CTTTTAGAGG TTGCAGAATC 780
TTACATGTGC TATAAACCAA GGACACACCC TACCCAAAAT TTATATACAC ATTCATGCAA 840
AATGTGTCAT GCAATCTCAG GGTTTCATGG AACCCGCTGA CACCCAGTCA TGGGCTCCTG 900
GCAATGAATT CCTGATCTCT GGGCTCTATT TGTCTAATAA TTCTATGAAA TATGTTTCTT 960
CCAAATTCTA TACTCCCCAC ACCCTCCATA AAATCATTTT TTAAAACATT TTTTTGTCTT 1020
CATTTATTTA AGAAACATTT ATTGAGTGCT ACCCACTCCT GTGGAAAAGT CCAGTATTGC 1080
TGGGAGAGAG AAAAGAGGAA AGGCCTCCAC CTGGGGTGTC TGCAAGAAGG GCACGGACAT 1140
TGGAGGTGCA GATGCACTGA AGAACTGATG GGCAAGCAAG ATAGATGGTC AAGGTTGGCA 1200
CTCAGAGGGG TGACCGTTAC CCGCCCCTCC ACCCCTTTCC CCGGCTTGTT GTAAGGGCAA 1260
GATCCTTCCC TCAACTCCAG AAATGAGTCA TCATGTGTCT ATGCCAGCCC TGGCAATCCC 1320
ATTCCCCTTT TTGAGTGTTT CCAACCCCAG TTTTGGACAA AGAGACCTAA GGGAAGTCAG 1380
TGTGCGACCC TCAATTCCTA GAAAAAAGAC AGAGCCTCAG AAAGAAAAGG CTTTTGGGCT 1440
GGATTACAGG 1450
|
